Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Slc9a5 ENSRNOG00000028844

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Description

solute carrier family 9 member A5 [Source:RGD Symbol;Acc:620473]

Gene Synonyms

NHE-5, Nhe5

Location

Primary_assembly 19: 50,136,740-50,156,827 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant), 190 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000068299.3	Slc9a5-201	4149	898aa	ENSRNOP00000063061.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9Z0X2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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